Reference Ranges for the Cough Responsiveness to Inhaled Mannitol

Cough Clinical Trial

Official title:

Reference Ranges for the Cough Responsiveness to Inhaled Mannitol

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05034367
• Other study ID #: 5801151
• Status: Recruiting
• Phase: N/A
• Start date: January 17, 2022
• Est. completion date: December 2024

Study information

• Verified date: March 2023
• Source: Kuopio University Hospital
• Contact: Heikki O Koskela, MD
• Phone: +358 447172795
• Email: heikki.koskela[@]kuh.fi
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cough is the most common reason why people seek medical attention in developed countries. The main mechanisms for prolonged cough are hypersensitivity of the cough reflex arc, sputum production, and constriction of the airway smooth muscles. Recognition of the mechanism in each cough patient is essential for the efficient management of prolonged cough. At present, there are no feasible tests for everyday clinical work to recognize cough reflex arc hypersensitivity.

Mannitol test was originally developed for asthma diagnostics. We have recently shown that it can also be used to investigate hypersensitive cough reflex arc. The purpose of the present study is to create reference ranges for normal cough responsiveness to inhaled mannitol. Without them, the test cannot be utilized in everyday clinical work. For that purpose we will perform mannitol test in 140 subjects, who are at least 18 years old and without any chronic respiratory symptoms or disorders. The subjects will be recruited in three centers: University of Eastern Finland and: John Hunter Hospital in Australia.The material will be collected 1.9.2021-31.12.2023. We apply funding for both personnel and material expences, to carry out this study.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 140
• Est. completion date: December 2024
• Est. primary completion date: December 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• age 18 years or older

• capable to understand the purpose of the study

• female/male ratio approximately 50%/50% in both of the following age groups:

• 50% aged 18- 50 yrs, and 50 % aged 51 - 90 years

Exclusion Criteria:

• Current daily smoking

• Ex-smoking with a greater than 10 pack years' daily smoking history or with stopping of daily smoking less than one year ago

• Pregnancy and breastfeeding

• A doctor's diagnosis of any respiratory diseases, including both upper and lower airway diseases, lung parenchymal diseases and the sleep apnoea syndrome

• A doctor's diagnosis of gastro-oesophageal reflux disease or symptoms suggestive of it

• Current use of angiotensin-converting enzyme inhibitors

• Upper respiratory tract infection ('flu') within 4 weeks

• Any current (within 4 weeks) cough 8

• Chronic (over 2 months' duration) cough during the last 12 months

• Wheezing during the last 12 months

• Attacks of shortness of breath or cough at night during the last 12 months

• Symptoms of rhinitis in a prolonged fashion during the last 12 months

• Heartburn or regurgitation once a week or more often during the last 3 months

• Abnormal anatomy of the respiratory organs, which may affect the deposition of the mannitol powder

• Any previous operations to the respiratory organs that can affect the deposition of the mannitol powder

• Unable to provide written informed consent to participate in the study

Related Conditions & MeSH terms

• Cough

Intervention

Diagnostic Test:
• Mannitol challenge
Inhalation challenge with dry powder of mannitol with a maximal cumulative dose of 635 mg

Locations

Country	Name	City	State
Australia	John Hunter Hospital	Newcastle	New South Wales
Finland	Kuopio University Hospital	Kuopio

Sponsors (2)

Lead Sponsor	Collaborator
Kuopio University Hospital	John Hunter Hospital

Countries where clinical trial is conducted

Australia,  Finland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cough-to-dose ratio	calculated as the number of coughs per 100 mg of total cumulative dose of mannitol	Coughs are recorded during the 60 seconds after each mannitol dose